WormBase Tree Display for Variation: WBVar01690351

WBVar01690351 Name: Public_name: WBVar01690351
    Other_name (11)
    HGVSg: CHROMOSOME_X:g.11232207G>A
  Sequence_details: SMap: S_parent: Sequence: C34F6
    Flanking_sequences: ACGATCATAGTTAACCTTACGATGATCATC CTATACTGTCGGAAGCGTGAAGGATGTTCA
    Mapping_target: C34F6
    Source_location: 225 CHROMOSOME_X 11232142 11232142 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00007944
    Transcript: C34F6.10a.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C34F6.10a.2:c.2412C>T
        HGVSp: CE43927:p.Ser804=
        cDNA_position: 2430
        CDS_position: 2412
        Protein_position: 804
        Exon_number: 8/17
        Codon_change: agC/agT
        Amino_acid_change: S
      C34F6.10d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C34F6.10d.1:c.2340C>T
        HGVSp: CE41362:p.Ser780=
        cDNA_position: 2474
        CDS_position: 2340
        Protein_position: 780
        Exon_number: 8/17
        Codon_change: agC/agT
        Amino_acid_change: S
      C34F6.10c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C34F6.10c.1:c.2358C>T
        HGVSp: CE53096:p.Ser786=
        cDNA_position: 2374
        CDS_position: 2358
        Protein_position: 786
        Exon_number: 7/16
        Codon_change: agC/agT
        Amino_acid_change: S
      C34F6.10b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C34F6.10b.1:c.2430C>T
        HGVSp: CE53121:p.Ser810=
        cDNA_position: 2455
        CDS_position: 2430
        Protein_position: 810
        Exon_number: 8/17
        Codon_change: agC/agT
        Amino_acid_change: S
      C34F6.10d.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C34F6.10d.2:c.2340C>T
        HGVSp: CE41362:p.Ser780=
        cDNA_position: 2358
        CDS_position: 2340
        Protein_position: 780
        Exon_number: 7/16
        Codon_change: agC/agT
        Amino_acid_change: S
      C34F6.10a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C34F6.10a.1:c.2412C>T
        HGVSp: CE43927:p.Ser804=
        cDNA_position: 2552
        CDS_position: 2412
        Protein_position: 804
        Exon_number: 9/18
        Codon_change: agC/agT
        Amino_acid_change: S
  Method: WGS_Flibotte